Human (GRCh38.p14)
Description

chromosome 22 open reading frame 39 [Source:HGNC Symbol;Acc:HGNC:27012]

Gene Synonyms

MGC74441

Location
About this transcript

This transcript has 3 exons, is annotated with 2 domains and features, is associated with 3102 variant alleles and maps to 318 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000399562.9C22orf39-2013720105aaENSP00000382474.5
 
Protein coding
CCDS33599Q6P5X5 NM_173793.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000399568.5C22orf39-202100580aaENSP00000382478.1
 
Protein coding
CCDS54498A0A075B6P1 -GENCODE basicTSL:1
ENST00000509549.5C22orf39-203297992aaENSP00000424903.1
 
Nonsense mediated decay
E0CX16 -TSL:2
Statistics

Exons: 3, Coding exons: 3, Transcript length: 3,720 bps, Translation length: 105 residues

MANE

This MANE Select transcript contains ENSP00000382474 and matches to NM_173793.5 and NP_776154.4

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q6P5X5

CCDS

This transcript is a member of the Human CCDS set: CCDS33599

Transcript Support Level (TSL)

TSL:1

Version

ENST00000399562.9

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Annotation Attributes

upstream ATG [Definitions]

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.